Propper Mfg. Co., Inc.
FDA 510(k) & PMA Approved Devices — 25 products
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Total Devices25
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111453 | STEAM DOT BLU PROCESS INDICATOR | JOJ | 2012-04-05 | View |
| 510(k) | K102894 | CLASSIX CHEMICAL STERILIZATION INDICATOR | JOJ | 2011-05-25 | View |
| 510(k) | K082620 | ONCE-A-DAY VERTOS TEST PACK | JOJ | 2009-07-08 | View |
| 510(k) | K031152 | PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) | JOJ | 2004-08-17 | View |
| 510(k) | K991618 | BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR | FRC | 2001-01-24 | View |
| 510(k) | K991276 | PASS/FAIL CHALLENGE PACK | JOJ | 1999-07-12 | View |
| 510(k) | K973585 | PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR | JOJ | 1998-11-06 | View |
| 510(k) | K972747 | BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) | FRC | 1998-01-09 | View |
| 510(k) | K961156 | ONCE-A-DAY BOWIE AND DICK TEST PACK. | JOJ | 1997-04-01 | View |
| 510(k) | K921798 | PROPPER SUPER SERACULT(R) | KHE | 1992-10-05 | View |
| 510(k) | K915804 | PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. | CCW | 1992-03-20 | View |
| 510(k) | K903024 | BI-O.K. STEAM TEST-PAK | FRC | 1990-09-12 | View |
| 510(k) | K895910 | STEAMLINE | JOJ | 1990-08-22 | View |
| 510(k) | K891784 | BI-O.K.(TM)-BIOLOGICAL/CHEMICAL INDICATOR | FRC | 1990-02-09 | View |
| 510(k) | K871672 | STERILIZATION INDICATOR FOR FLASH STERILIZATION | LRT | 1987-06-01 | View |
| 510(k) | K851804 | BIO-CHALLENGE TEST PAK | JOJ | 1985-07-16 | View |
| 510(k) | K834353 | OK FLASH STERILIZATION INDICATOR | JOJ | 1984-03-19 | View |
| 510(k) | K834297 | PROPPER SERACULT | KHE | 1984-01-27 | View |
| 510(k) | K821648 | GAS CHEX PLASTIC BAG | JOJ | 1982-06-22 | View |
| 510(k) | K813204 | SERACULT OCCULT BLOOF TEST | KHE | 1982-01-28 | View |
No matching devices.
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